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Journal of Inherited Metabolic Disease|September 22, 2006
Large neutral amino acids in the treatment of phenylketonuria (PKU)R Matalon, K Michals-Matalon, G Bhatia, et al.Journal of Inherited Metabolic Disease|October 27, 2004
Maternal Phenylketonuria Collaborative Study (MPKUCS)--the 'outliers'W B Hanley, C Azen, R Koch, et al.Pediatric Research|August 1, 1989
Effects of ascorbic acid in alkaptonuria: alterations in benzoquinone acetic acid and an ontogenic effect in infancyJ A Wolff, B Barshop, W L Nyhan, et al.International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|January 1, 1976
Prenatal diagnosis of inborn errors of metabolismR MatalonFrontiers in Bioscience : a Journal and Virtual Library|March 8, 2000
Spongy degeneration of the brain, Canavan disease: biochemical and molecular findingsR M Matalon, K Michals-MatalonJournal of the American Dietetic Association|November 1, 1978
Dietary treatment of tyrosinemia type I: importance of methionine restrictionK Michals, R Matolon, P W WongProceedings of the National Academy of Sciences of the United States of America|February 1, 1976
The mucopolysaccharidoses (a review)A Dorfman, R MatalonAmerican Journal of Public Health|January 1, 1985
Reinstitution of diet therapy in PKU patients from twenty-two US clinicsV E Schuett, E S Brown, K MichalsThe Journal of Clinical Investigation|October 1, 1974
Sanfilippo A syndrome: sulfamidase deficiency in cultured skin fibroblasts and liverR Matalon, A DorfmanPageof 12